Impact of a Checklist on the Rate of Late Cancellation in Ambulatory Surgery

NCT ID: NCT01732159

Last Updated: 2015-04-21

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

4093 participants

Study Classification

INTERVENTIONAL

Study Start Date

2012-11-30

Study Completion Date

2014-04-30

Brief Summary

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The purpose of this study is to evaluate the impact of a check list on the rate of late cancellation, i.e. the day before or the day of the ambulatory surgery.

Detailed Description

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The checklist is administered to the patients by phone between 7 and 3 days before the surgery. Each item of the checklist is associated with a decisional algorithm that allows take care for patients in case of any problem.

Conditions

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Ambulatory Surgery Programmed

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Blinding Strategy

NONE

Study Groups

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Administration of the checklist

Patients will be contacted by phone for administration of the checklist

Group Type EXPERIMENTAL

Checklist

Intervention Type OTHER

he checklist will be administered to the patients by phone between 7 and 3 days before the surgery

No contact by phone

Patients who will not be contacted by phone

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Checklist

he checklist will be administered to the patients by phone between 7 and 3 days before the surgery

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patient (adult or minor) for which ambulatory surgery is programmed in a multipurpose ASU
* Surgery under general anesthesia or loco
* Regional or neuroleptanalgesia3. Patient contacted by phone
* Patient does not oppose his participation in the study

Exclusion Criteria

* Patient programmed for endoscopy in ASU non surgical
* Ambulatory surgery scheduled for orthogenic
* Ambulatory surgery scheduled for urgency
* Ambulatory surgery performed under local anesthesia
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Assistance Publique - Hôpitaux de Paris

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Jean-Pierre BETHOUX, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Cochin Hospital

Locations

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Cochin Hospital

Paris, , France

Site Status

Countries

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France

References

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Gaucher S, Boutron I, Marchand-Maillet F, Baron G, Douard R, Bethoux JP; AMBUPROG Group Investigators. Assessment of a Standardized Pre-Operative Telephone Checklist Designed to Avoid Late Cancellation of Ambulatory Surgery: The AMBUPROG Multicenter Randomized Controlled Trial. PLoS One. 2016 Feb 1;11(2):e0147194. doi: 10.1371/journal.pone.0147194. eCollection 2016.

Reference Type DERIVED
PMID: 26829478 (View on PubMed)

Other Identifiers

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K110601

Identifier Type: -

Identifier Source: org_study_id

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